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10.3390/ijms19020546

http://scihub22266oqcxt.onion/10.3390/ijms19020546
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C5855768!5855768!29439489
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suck abstract from ncbi


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pmid29439489      Int+J+Mol+Sci 2018 ; 19 (2): ä
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  • The Low-Renin Hypertension Phenotype: Genetics and the Role of the Mineralocorticoid Receptor #MMPMID29439489
  • Baudrand R; Vaidya A
  • Int J Mol Sci 2018[Feb]; 19 (2): ä PMID29439489show ga
  • A substantial proportion of patients with hypertension have a low or suppressed renin. This phenotype of low-renin hypertension (LRH) may be the manifestation of inherited genetic syndromes, acquired somatic mutations, or environmental exposures. Activation of the mineralocorticoid receptor is a common final mechanism for the development of LRH. Classically, the individual causes of LRH have been considered to be rare diseases; however, recent advances suggest that there are milder and ?non-classical? variants of many LRH-inducing conditions. In this regard, our understanding of the underlying genetics and mechanisms accounting for LRH, and therefore, potentially the pathogenesis of a large subset of essential hypertension, is evolving. This review will discuss the potential causes of LRH, with a focus on implicated genetic mechanisms, the expanding recognition of non-classical variants of conditions that induce LRH, and the role of the mineralocorticoid receptor in determining this phenotype.
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